—#47858

Product

Zimmer ZMR Hip System femoral body, revision, nitrided, porous, 12/14 neck taper, standard, 40 mm neck offset, cone body, size C, 45 mm build-up, tivanium TI-6AL-4V alloy, sterile; REF. 9996-19-45 (Cat. no. 00999601945).

FDA product code: LPH — Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Device class: Class 2
Medical specialty: Orthopedic
510(k) numbers: K994286
Affected lot / code info: Lot 60451050.

Why it was recalled

Lack of assurance of proper metal fatigue strength due to a metal grain structure anomaly.

Root cause (FDA determination)

Other

Action the firm took

Consignees were notified via letter dated 8/2/06 to cease use of and to return the products. Zimmer distributors were to examine stock and return product on hand.

Recalling firm

Firm: Zimmer Inc.
Address: 345 E Main St, Warsaw, Indiana 46580-2746

Distribution

Distribution pattern: Worldwide, including USA, Australia, China, Denmark, Japan, Jordan, Latin Ameria, Russia, Singapore and Switzerland.

Timeline

Recall initiated: 2006-08-02
Posted by FDA: 2006-08-31
Terminated: 2007-05-04
Status: —

Source: openFDA Device Recall endpoint. Recall record ID #47858. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.